Canonical Allele Identifier: CA1786790593

Gene: FAM110B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.58073997C= , CM000670.2:g.58073997C=	GRCh38
NC_000008.10:g.58986556C= , CM000670.1:g.58986556C=	GRCh37
NC_000008.9:g.59149110C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519262.6:c.-413-1538C= MANE Select	ENSP00000509301.1:n.-413-1538C=
ENST00000361488.7:c.-413-1538C=	ENSP00000355204.3:n.-413-1538C=
ENST00000518427.5:n.182-1538C=
ENST00000519262.5:n.397-1538C=
ENST00000520369.5:n.338-1538C=
ENST00000521413.1:n.46-1538C=
ENST00000522059.5:n.89-1538C=
ENST00000523486.5:n.137-1538C=
NM_147189.2:c.-413-1538C=	NP_671722.1:n.-413-1538C=
XM_005251324.1:c.-413-1538C=	XP_005251381.1:n.-413-1538C=
XM_005251325.2:c.-413-1538C=	XP_005251382.1:n.-413-1538C=
XM_005251326.1:c.-413-1538C=	XP_005251383.1:n.-413-1538C=
XM_005251324.3:c.-413-1538C=	XP_005251381.1:n.-413-1538C=
XM_005251325.3:c.-413-1538C=	XP_005251382.1:n.-413-1538C=
XM_005251326.3:c.-413-1538C=	XP_005251383.1:n.-413-1538C=
XM_017013948.1:c.-413-1538C=	XP_016869437.1:n.-413-1538C=
NM_147189.3:c.-413-1538C=	NP_671722.1:n.-413-1538C=
NM_001377989.1:c.-413-1538C= MANE Select	NP_001364918.1:n.-413-1538C=
NM_001377997.1:c.-413-1538C=	NP_001364926.1:n.-413-1538C=
NM_001377998.1:c.-413-1538C=	NP_001364927.1:n.-413-1538C=
NM_147189.4:c.-413-1538C=	NP_671722.1:n.-413-1538C=